OPENING OF 2',3'-O-ANHYDRO-RING OF 2',3'-O-ANHYDRO-LYXO-URIDINE BY ALKYLAMINES AND ARYLAMINES - EASY SYNTHESES AND PREPARATIVE USES OF 2'-DEOXY-2'-ALKYLAMINO-XYLO-URIDINES AND 3'-DEOXY-3'-ALKYLAMINO-ARA-URIDINES

被引:9
作者
BERA, S
PATHAK, T
LANGLEY, GJ
机构
[1] NATL CHEM LAB, DIV ORGAN CHEM SYNTH, POONA 411008, MAHARASHTRA, INDIA
[2] UNIV SOUTHAMPTON, DEPT CHEM, SOUTHAMPTON SO9 5NH, HANTS, ENGLAND
关键词
D O I
10.1016/0040-4020(94)01040-7
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Contrary to the previous report (ref. 8), under controlled conditions alkylamines, both primary and secondary and arylamines, opened the epoxide ring of 1-(5-0-trityl-2,3-O-anhydro-beta-D-lyxo-furanosyl)-uracil to produce 2'-deoxy-2'-alkylamino-xylo- and 3'-deoxy-3'-alkylaminoara- uridines without causing any significant deglycosylation. To show tire utility of these products, several modified uridine derivatives were synthesised.
引用
收藏
页码:1459 / 1470
页数:12
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